Analyzing bleeding during laparoscopic pancreatic surgery
Analysis of Intraoperative Bleeding Characteristics in Laparoscopic Pancreaticoduodenectomy
This study looks at how different surgical techniques during laparoscopic pancreatic surgery affect bleeding and how that bleeding impacts recovery for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 400 (estimated) |
| Sex | All |
| Sponsor | West China Hospital Academic / other |
| Locations | 1 site (Chengdu, Sichuan) |
| Trial ID | NCT06128603 on ClinicalTrials.gov |
What this trial studies
This study examines the bleeding characteristics that occur during laparoscopic pancreaticoduodenectomy by reviewing and annotating surgical videos. It focuses on the correlation between surgical techniques, as assessed by OSATS scores, and the incidence of intraoperative bleeding. Additionally, the study aims to explore how intraoperative bleeding impacts short-term postoperative outcomes. By analyzing these factors, the research seeks to enhance surgical practices and patient safety.
Who should consider this trial
Good fit: Ideal candidates for this study are patients undergoing laparoscopic pancreaticoduodenectomy with complete surgical video documentation.
Not a fit: Patients whose surgical videos are incomplete or who have undergone combined resection and reconstruction of the mesentericoportal vein may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical techniques that minimize intraoperative bleeding and enhance patient recovery.
How similar studies have performed: While this approach is observational and builds on existing surgical practices, similar studies have shown that analyzing surgical techniques can lead to improved outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * the surgical video is complete including the resection and reconstruction phases Exclusion Criteria: * the surgical video is not complete * the cases combined with resection and reconstruction of mesentericoportal vein
Where this trial is running
Chengdu, Sichuan
- West China Hospital of Sichuan University — Chengdu, Sichuan, China (Recruiting)
Study contacts
- Study coordinator: He Cai, MD.
- Email: 813021545@qq.com
- Phone: +862862539242
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.